A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514509



Internal ID20887863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41226702..41255418hg38UCSC Ensembl
chr17:39382954..39411670hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3828717
hg1928717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035480
Samples
Known GenesKRTAP9-2, KRTAP9-3, KRTAP9-4, KRTAP9-8, KRTAP9-9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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